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Team:Fatih-Medical/Sherlocoli/Results
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<map id="imgmap201292735814" name="imgmap201292735814"><area shape="rect" alt="" title="" coords="152,207,275,249" href="https://2012.igem.org/Team:Fatih-Medical/Sherlocoli" target="" /><area shape="rect" alt="" title="" coords="279,208,398,250" href="https://2012.igem.org/Team:Fatih-Medical/Sherlocoli/Goals" target="" /><area shape="rect" alt="" title="" coords="404,208,515,248" href="https://2012.igem.org/Team:Fatih-Medical/Sherlocoli/Design" target="" /><area shape="rect" alt="" title="" coords="523,208,641,249" href="https://2012.igem.org/Team:Fatih-Medical/Sherlocoli/Assembly" target="" /><area shape="rect" alt="" title="" coords="645,207,765,248" href="https://2012.igem.org/Team:Fatih-Medical/Sherlocoli/Modelling" target="" /><area shape="rect" alt="" title="" coords="773,208,887,247" href="https://2012.igem.org/Team:Fatih-Medical/Sherlocoli/Results" target="" /><!-- Created by Online Image Map Editor (http://www.maschek.hu/imagemap/index) --></map> | <map id="imgmap201292735814" name="imgmap201292735814"><area shape="rect" alt="" title="" coords="152,207,275,249" href="https://2012.igem.org/Team:Fatih-Medical/Sherlocoli" target="" /><area shape="rect" alt="" title="" coords="279,208,398,250" href="https://2012.igem.org/Team:Fatih-Medical/Sherlocoli/Goals" target="" /><area shape="rect" alt="" title="" coords="404,208,515,248" href="https://2012.igem.org/Team:Fatih-Medical/Sherlocoli/Design" target="" /><area shape="rect" alt="" title="" coords="523,208,641,249" href="https://2012.igem.org/Team:Fatih-Medical/Sherlocoli/Assembly" target="" /><area shape="rect" alt="" title="" coords="645,207,765,248" href="https://2012.igem.org/Team:Fatih-Medical/Sherlocoli/Modelling" target="" /><area shape="rect" alt="" title="" coords="773,208,887,247" href="https://2012.igem.org/Team:Fatih-Medical/Sherlocoli/Results" target="" /><!-- Created by Online Image Map Editor (http://www.maschek.hu/imagemap/index) --></map> | ||
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<b>• EpCAM binding docks are cloned and confirmed.</b> | <b>• EpCAM binding docks are cloned and confirmed.</b> | ||
| - | The gene sequences of EpCAM binding docks are synthesized particularly and separately. [See details] The confirmation electrophoresis and PCR afterwards were found correct. [See | + | The gene sequences of EpCAM binding docks are synthesized particularly and separately. [See details] The confirmation electrophoresis and PCR afterwards were found correct. [See Image] BBa_K772001 and BBa_K772002 are fixed together via 3A assembly method. After transformation into E.coli, the gel bands match with their original length; therefore we proceeded to the next step: Sequencing.<br><br> |
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| + | <img src="https://static.igem.org/mediawiki/igem.org/archive/e/e0/20120927030036!20120925_161036.jpg"><br><br> | ||
| + | <img src="https://static.igem.org/mediawiki/igem.org/archive/e/e0/20120927030055!20120925_161036.jpg"><br><br> | ||
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<b>• Binding docks are sequenced and found correct.</b> | <b>• Binding docks are sequenced and found correct.</b> | ||
Sequence results overlap with the original sequences and show that these two parts are assembled correctly and ready to test for the synthesis and its function. <br><br> | Sequence results overlap with the original sequences and show that these two parts are assembled correctly and ready to test for the synthesis and its function. <br><br> | ||
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| + | <img src="https://static.igem.org/mediawiki/2012/c/c5/Sekans.png"> | ||
<b>• Binding docks are synthesized and are able to bind to the EpCAM.</b> | <b>• Binding docks are synthesized and are able to bind to the EpCAM.</b> | ||
After the correct ligation and cloning procedures, we extracted both bacterial and tumor cell protein ingredients via performing sonication. Affinity Gel Chromatography is performed on bacterial protein extract in order to isolate our EpCAM binding docks. These docks were exposed to tumor cell extract; thus the binding would occur. SDS-PAGE is done aftermath on the last solution. <br><br> | After the correct ligation and cloning procedures, we extracted both bacterial and tumor cell protein ingredients via performing sonication. Affinity Gel Chromatography is performed on bacterial protein extract in order to isolate our EpCAM binding docks. These docks were exposed to tumor cell extract; thus the binding would occur. SDS-PAGE is done aftermath on the last solution. <br><br> | ||
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| + | <img style="float: left; margin: 10px; width: 200px;" src="https://static.igem.org/mediawiki/2012/archive/f/f7/20120927035038!Sherlocoli_Overview_%281%29.png"> | ||
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| + | <img style="float: left; margin: 10px; width: 600px;" src="https://static.igem.org/mediawiki/igem.org/archive/e/e0/20120927030300!20120925_161036.jpg"><br><br> | ||
</div> | </div> | ||
Latest revision as of 04:00, 27 September 2012
• EpCAM binding docks are cloned and confirmed. The gene sequences of EpCAM binding docks are synthesized particularly and separately. [See details] The confirmation electrophoresis and PCR afterwards were found correct. [See Image] BBa_K772001 and BBa_K772002 are fixed together via 3A assembly method. After transformation into E.coli, the gel bands match with their original length; therefore we proceeded to the next step: Sequencing.
• Binding docks are sequenced and found correct. Sequence results overlap with the original sequences and show that these two parts are assembled correctly and ready to test for the synthesis and its function.
• Binding docks are synthesized and are able to bind to the EpCAM.
After the correct ligation and cloning procedures, we extracted both bacterial and tumor cell protein ingredients via performing sonication. Affinity Gel Chromatography is performed on bacterial protein extract in order to isolate our EpCAM binding docks. These docks were exposed to tumor cell extract; thus the binding would occur. SDS-PAGE is done aftermath on the last solution. 
